| CAS No. | 119963-50-7 |
| Molecular Formula | C19H16O3 |
| Molecular Weight | 292.33 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Compared with other compounds in its class, the molecular weight of 292.33 g/mol gives 1,6,6-Trimethyl-6,7-dihydrophenanthro[1,2-b]furan-10,11-dione distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
CATO supplies 1,6,6-Trimethyl-6,7-dihydrophenanthro[1,2-b]furan-10,11-dione (CAS 119963-50-7), a certified reference material (molecular formula C19H16O3, MW 292.33 g/mol) for analytical method development and quality control.
The molecular framework of 1,6,6-Trimethyl-6,7-dihydrophenanthro[1,2-b]furan-10,11-dione (C19H16O3) is characterized by a steroid core, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).
This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.
As a certified reference material (CRM), 1,6,6-Trimethyl-6,7-dihydrophenanthro[1,2-b]furan-10,11-dione meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.
| Molecular Formula | C19H16O3 |
| Molecular Weight | 292.33 g/mol |
| Appearance | Pale yellow to yellow crystalline powder |
| Purity | 97%+ |
| Storage | Store at 2-8°C, protect from light, keep sealed and dry |
| Solubility (reference) | Soluble in chloroform, dichloromethane, ethyl acetate, DMSO |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | 12.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1991 |